Fig. 6
From: Proteomic profiling of liver tissue from the mdx-4cv mouse model of Duchenne muscular dystrophy
Overview of the proteomic identification of the fatty acid binding protein FABP5 in liver tissue extracts from the mdx-4cv mouse model of dystrophinopathy. Shown is the potential correlation between primary skeletal muscle abnormalities in X-linked muscular dystrophy and secondary changes in liver metabolism, as well as an overview of affected biochemical pathways in the mdx-4cv liver as determined by LS-MS/MS analysis. The mass spectrometric fingerprint of the most increased protein species in the mdx-4cv liver, FABP5, is shown and a comparative sequence alignment with other members of the FABP family to illustrate the uniqueness of the identifying peptide sequence of FABP5